Analysis performed by the NRC
- Confirmation of bacterial identification to species level using MALDI-TOF MS
- Screening of antimicrobial resistance mechanisms by in vitro susceptibility testing to 16 antimicrobial drugs using disc diffusion
- Determination of MICs by broth microdilution method according the EUCAST guidelines and interpretative breakpoints
- Carbapenem hydrolysis-based tests
- Inhibitors-based combination disk tests:
- For the detection of ESBL and/or hyperproduced AmpC
- For the detection of carbapenemase
- Extended susceptibility disk diffusion testing against aminoglycosides for the detection of 16S rRNA methylases
- Immunochromatographic detection of carbapenemase (OXA-48, KPC, VIM, NDM and OXA-23)
- End-point PCR simplex or multiplex targetting
- Class A and class B carbapenemases (NDM, VIM, KPC, IMP, IMI, SIM, GIM, DIM, FIM, SMB, SME, SPM)
- Class D carbapenemases (OXA-48, OXA-427, OXA-198, OXA-23, OXA-24, OXA-58)
- Major ESBL families (TEM, SHV and PME )
- minor ESBL families (GES, VEB, PER and BEL)
- oxacillinase group (OXA-1,OXA-2,OXA-9,OXA-10, OXA-18,OXA-20)
- 16S rRNA methylases (ArmA, Rmt A-B-C-D-E-F-G, NpmA)
- plasmid-borne quinolone resistance genes (QnrA, QnrB, QnrS)
- Other genetic characterization methods:
- Sequencing of resistance genes and the genetic environment by NGS
- Plasmid extraction by Kieser method
- Conjugation, transformation and cloning
- PCR-based replicon typing : method based on replicons (Inc/rep PCR) of the major plasmid incompatibility groups (Caratolli A. et al , JAC. 2010 Dec;65(12):2518-29)
Serotyping of Pseudomonas eruginosa by NGS
MLST typing : sequencing of 7 house keeping genes and definition of ST according the website
core MLST typing: sequencing of 629 house keeping genes and definition of cgST according the website
A. baumannii : http://pubmlst.org/abaumannii
P. aeruginosa : http://pubmlst.org/paeruginosa